Linked Data
MyVariant Identifiers:
chr19:g.9325253T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.9214577T>G , CM000681.2:g.9214577T>G | GRCh38 |
| NC_000019.9:g.9325253T>G , CM000681.1:g.9325253T>G | GRCh37 |
| NC_000019.8:g.9186253T>G | NCBI36 |
| NG_027953.1:g.5295A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000641244.1:c.261A>C | ENSP00000493404.1:p.Ala87= | |
| ENST00000641669.1:c.261A>C MANE Select | ENSP00000493383.1:p.Ala87= | |
| ENST00000308682.3:c.261A>C | ENSP00000310488.2:p.Ala87= | |
| NM_001005191.2:c.261A>C | NP_001005191.1:p.Ala87= | |
| NM_001005191.3:c.261A>C MANE Select | NP_001005191.1:p.Ala87= |